Acute Human Self-Poisoning with Imidacloprid Compound: A Neonicotinoid Insecticide

被引:98
作者
Mohamed, Fahim
Gawarammana, Indika
Robertson, Thomas A.
Roberts, Michael S.
Palangasinghe, Chathura
Zawahir, Shukry
Jayamanne, Shaluka
Kandasamy, Jaganathan
Eddleston, Michael
Buckley, Nick A.
Dawson, Andrew H.
Roberts, Darren M.
机构
[1] South Asian Clinical Toxicology Research Collaboration, Department of Clinical Medicine, University of Peradeniya, Peradeniya
[2] Therapeutics Research Unit, School of Medicine, University of Queensland, Brisbane, QLD
[3] Polonnaruwa General Hospital, North Central Province, Polonnaruwa
[4] Anuradhapura General Hospital, North Central Province, Anuradhapura
[5] Scottish Poisons Information Bureau, Royal Infirmary of Edinburgh, University of Edinburgh, Edinburgh
[6] Medical Professorial Unit, POW Hospital Clinical School, University of New South Wales, Kensington, NSW
[7] School of Medicine and Public Health, University of Newcastle, Callaghan, NSW
[8] Burns Trauma and Critical Care Research Centre, University of Queensland, Brisbane, QLD
基金
英国惠康基金;
关键词
D O I
10.1371/journal.pone.0005127
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Deliberate self-poisoning with older pesticides such as organophosphorus compounds are commonly fatal and a serious public health problem in the developing world. The clinical consequences of self-poisoning with newer pesticides are not well described. Such information may help to improve clinical management and inform pesticide regulators of their relative toxicity. This study reports the clinical outcomes and toxicokinetics of the neonicotinoid insecticide imidacloprid following acute self-poisoning in humans. Methodology/Principal Findings: Demographic and clinical data were prospectively recorded in patients with imidacloprid exposure in three hospitals in Sri Lanka. Blood samples were collected when possible for quantification of imidacloprid concentration. There were 68 patients (61 self-ingestions and 7 dermal exposures) with exposure to imidacloprid. Of the self-poisoning patients, the median time to presentation was 4 hours (IQR 2.3-6.0) and median amount ingested was 15 mL (IQR 10-50 mL). Most patients only developed mild symptoms such as nausea, vomiting, headache and diarrhoea. One patient developed respiratory failure needing mechanical ventilation while another was admitted to intensive care due to prolonged sedation. There were no deaths. Median admission imidacloprid concentration was 10.58 ng/L; IQR: 3.84-15.58 ng/L, Range: 0.02-51.25 ng/L. Changes in the concentration of imidacloprid in serial blood samples were consistent with prolonged absorption and/or saturable elimination. Conclusions: Imidacloprid generally demonstrates low human lethality even in large ingestions. Respiratory failure and reduced level of consciousness were the most serious complications, but these were uncommon. Substitution of imidacloprid for organophosphorus compounds in areas where the incidence of self-poisoning is high may help reduce deaths from self-poisoning.
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页数:5
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